Transcriptional expression of RPMS1 in nasopharyngeal carcinoma and its oncogenic potential

Cell Cycle. 2005 Feb;4(2):304-9. Epub 2005 Feb 17.

Abstract

The Epstein-Barr virus (EBV) BamHI A rightward transcripts (BARTs) were originally identified in C15 xenograft of nasopharyngeal carcinoma (NPC) and easily detected in a wide variety of EBV latent infection and EBV-associated tumors. It had been reported that p31 cosmid containing BARTs immortalized monkey epithelial cells, but which particular gene among BARTs family participates in the transformation procedure remains to be identified. RPMS1 is the only full-length cDNA confirmed so far and one of the most abundant spliced forms in BARTs family. To investigate the involvement of RPMS1 gene in NPC, we examined the expression of RPMS1 transcripts in NPC biopsies from Guangdong and its oncogenic potential. Our results revealed that RPMS1 mRNA preferentially expressed in primary NPC to non-carcinoma tissue of nasopharynx and peripheral blood lymphocytes (PBLs) of NPC patients. Furthermore, by introducing RPMS1 ORF into HEK293 cells, these transfectants enhanced the anchorage-independent growth and produced tumors in nude mice. These data imply that RPMS1 gene might play an important role in the development of NPC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Cell Transformation, Neoplastic / genetics*
  • Cell Transformation, Neoplastic / pathology
  • China / epidemiology
  • Gene Expression Regulation, Neoplastic*
  • Herpesvirus 4, Human* / genetics
  • Humans
  • Lymphocytes / chemistry
  • Lymphocytes / pathology
  • Mice
  • Mice, Nude
  • Microscopy, Confocal
  • Molecular Sequence Data
  • Nasopharyngeal Neoplasms / chemistry
  • Nasopharyngeal Neoplasms / epidemiology
  • Nasopharyngeal Neoplasms / genetics*
  • Nasopharyngeal Neoplasms / pathology
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / physiology
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • Transcription, Genetic*
  • Transfection
  • Viral Proteins / analysis
  • Viral Proteins / genetics*
  • Viral Proteins / physiology

Substances

  • Neoplasm Proteins
  • RNA, Messenger
  • RPMS protein, Human herpesvirus 4
  • Viral Proteins